Loss of Calretinin in L5a impairs the formation of the barrel cortex leading to abnormal whisker-mediated behaviors

Mol Brain. 2021 Apr 12;14(1):67. doi: 10.1186/s13041-021-00775-w.

Abstract

The rodent whisker-barrel cortex system has been established as an ideal model for studying sensory information integration. The barrel cortex consists of barrel and septa columns that receive information input from the lemniscal and paralemniscal pathways, respectively. Layer 5a is involved in both barrel and septa circuits and play a key role in information integration. However, the role of layer 5a in the development of the barrel cortex remains unclear. Previously, we found that calretinin is dynamically expressed in layer 5a. In this study, we analyzed calretinin KO mice and found that the dendritic complexity and length of layer 5a pyramidal neurons were significantly decreased after calretinin ablation. The membrane excitability and excitatory synaptic transmission of layer 5a neurons were increased. Consequently, the organization of the barrels was impaired. Moreover, layer 4 spiny stellate cells were not able to properly gather, leading to abnormal formation of barrel walls as the ratio of barrel/septum size obviously decreased. Calretinin KO mice exhibited deficits in exploratory and whisker-associated tactile behaviors as well as social novelty preference. Our study expands our knowledge of layer 5a pyramidal neurons in the formation of barrel walls and deepens the understanding of the development of the whisker-barrel cortex system.

Keywords: Barrel cortex; Calretinin; Exploratory behavior; Layer 5a pyramidal neurons; Lemniscal pathway; Paralemniscal pathway; Tactile sensation behavior.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Behavior, Animal / physiology*
  • Calbindin 2 / deficiency*
  • Calbindin 2 / metabolism
  • Cell Membrane / metabolism
  • Dendrites / metabolism
  • Exploratory Behavior
  • Gene Deletion
  • Mice
  • Mice, Knockout
  • Pyramidal Cells / metabolism
  • Sensation
  • Synaptic Transmission
  • Touch
  • Vibrissae / anatomy & histology*

Substances

  • Calbindin 2